The purpose of this proposal is to develop, validate and integrate novel biomarkers to characterize the risk of getting, having, or progressing with breast cancer. We have assembled a superb multidisciplinary team of academic and industry investigators who are using molecular and cell based technologies for biomarker development. We will further develop and evaluate them using powerful clinical resources, including unique retrospective and prospective data sets, and will integrate them with each other (cross validation) and into the context of clinical decision (modeling). The proposed studies attempt to redefine the paradigm from conventional breast cancer screening to combined detection/biological characterization/risk projection. Our hypotheses are that: 1) SNP (germline) and proteomic (serum) profiles can define breast cancer risk and detect early cancer, and may be combined for a tiered screening strategy; 2) Promising biomarkers indicative of risk of progression and metastasis, including tissue-based expression profiling and detection of circulating tumor cells (CTCs), should be directly compared as well as integrated to maximize information about phenotypes and risk; and 3) Combined analysis of biomarkers is not only more efficient but may lead to integrated strategies for optimal clinical application. In order to accomplish our work we propose 4 projects: Project 1: Develop SNP- and serum proteomics-based profiles for cancer detection (primary and secondary) and risk profiling in the context of clinical evaluation of palpable and mammographic abnormalities; Project 2: Develop paraffin based expression profiles to predict risk of disease progression using retrospective datasets (Guy's Hospital: natural history population with 25 yr follow-up and no systemic therapy; UCSF comprehensive micrometastases/CTC data set; UCSF SPORE DCIS data set); Project 3: Develop and validate CTC-based assays, including leading approaches for CTC detection; cross-validate CTC data with tissue-based biomarkers; and develop methods for molecular profiling of CTCs; Project 4: Evaluate promising biomarkers in a prospective clinical study for cross validation of assays and integration into predictive outcome models that reflect the biological properties of the cancer detected. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01CA111234-03
Application #
7121540
Study Section
Special Emphasis Panel (ZCA1-SRRB-E (O1))
Program Officer
Patriotis, Christos F
Project Start
2004-09-20
Project End
2009-07-31
Budget Start
2006-08-01
Budget End
2007-07-31
Support Year
3
Fiscal Year
2006
Total Cost
$812,190
Indirect Cost
Name
University of California San Francisco
Department
Surgery
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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Yau, Christina; Wang, Yixin; Zhang, Yi et al. (2011) Young age, increased tumor proliferation and FOXM1 expression predict early metastatic relapse only for endocrine-dependent breast cancers. Breast Cancer Res Treat 126:803-10
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Yau, Christina; Esserman, Laura; Moore, Dan H et al. (2010) A multigene predictor of metastatic outcome in early stage hormone receptor-negative and triple-negative breast cancer. Breast Cancer Res 12:R85

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